Canonical Allele Identifier: CA1955197746
Gene: OTOG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17553384G= , CM000673.2:g.17553384G= GRCh38
NC_000011.9:g.17574931G= , CM000673.1:g.17574931G= GRCh37
NC_000011.8:g.17531507G= NCBI36
NG_033191.1:g.11012G=
NG_033191.2:g.11012G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000399391.7:c.441G= ENSP00000382323.2:p.Glu147=
ENST00000399397.6:c.405G= MANE Select ENSP00000382329.2:p.Glu135=
ENST00000399391.6:c.441G= ENSP00000382323.2:p.Glu147=
ENST00000399397.5:c.405G= ENSP00000382329.2:p.Glu135=
ENST00000428619.1:c.222G= ENSP00000399057.2:p.Glu74=
ENST00000498332.5:n.311G=
NM_001277269.1:c.441G= NP_001264198.1:p.Glu147=
NM_001292063.1:c.405G= NP_001278992.1:p.Glu135=
NM_001277269.2:c.441G= NP_001264198.1:p.Glu147=
NM_001292063.2:c.405G= MANE Select NP_001278992.1:p.Glu135=